FDA Inspection 1201241 — Ajinomoto Omnichem NV

Ajinomoto Omnichem NV — FEI 3002807802

The FDA completed an inspection of Ajinomoto Omnichem NV on Mar 16, 2022 in Wetteren. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions or practices were found, but the agency is not prepared to take or recommend any administrative or regulatory action). Product area: Drugs.

Inspection details

Classification
Voluntary Action Indicated (VAI)
End Date
Mar 16, 2022
Fiscal Year
2022
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Wetteren (Belgium)

Additional details

Mutual Recognition Agreement (MRA)

Sources: openFDA, FDA Data Dashboard, FDA.gov. Report a data issue: hello@regdatalab.com.